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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00514670
Other study ID # 06-01-0014
Secondary ID
Status Completed
Phase N/A
First received August 9, 2007
Last updated August 9, 2007
Start date March 2006
Est. completion date May 2006

Study information

Verified date August 2007
Source Children's Hospital Boston
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The objective of the trial is to assess the impact of a disinfection and hand hygiene program on absenteeism in elementary school classrooms. Students in intervention classrooms will use alcohol-based hand sanitizers at school, and their classrooms will be disinfected using quaternary ammonium wipes. We hypothesize that the use of disinfectants and hand hygiene products in elementary school classrooms will reduce absenteeism.


Recruitment information / eligibility

Status Completed
Enrollment 285
Est. completion date May 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Member of a designated elementary school classroom in the Avon school system

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Intervention

Other:
Alcohol-based hand sanitizer & quaternary ammonium wipes


Locations

Country Name City State
United States Children's Hospital Boston Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Children's Hospital Boston Study funds provided by The Clorox Company

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Absenteeism rate due to gastrointestinal or respiratory illness during the study period. 8 weeks
Secondary Bacterial colony counts and the presence of selected viruses on classroom surfaces. 8 weeks
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